Trisomy of the short arm of chromosome 10.
- 1 December 1975
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 12 (4), 412-414
- https://doi.org/10.1136/jmg.12.4.412
Abstract
A case of a fetus with multiple malformations is described. The mother showed a 46,XX,rcp(10;22) (p11;p11) karyotype. Amniocentesis at the 16th wk of gestation revealed that the male fetus had a der(22) chromosome.sbd.that is, he was trisomic for a large part of 10p (10pter .fwdarw. 10p11). Clinical findings of cases with 10p, 10q, and mosaic 10 trisomies are briefly reviewed.This publication has 4 references indexed in Scilit:
- Trisomy 10 with mosaicism. A clinical and cytogenetic entity.1973
- G-group chromosomes in satellite associationsCytogenetic and Genome Research, 1973
- [A case of multiple congenital anomalies with familial C-G translocation].1970
- [Multiple malformations in partial trisomy C (12) as manifestation of an inherited E-C (18/12) translocation].1967